Papers associated with right (and grin2b)

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	A convergent molecular network underlying autism and congenital heart disease., Rosenthal SB., Cell Syst. November 17, 2021; 12 (11): 1094-1107.e6.
	Two de novo GluN2B mutations affect multiple NMDAR-functions and instigate severe pediatric encephalopathy., Kellner S., Elife. July 2, 2021; 10
	Functional limb muscle innervation prior to cholinergic transmitter specification during early metamorphosis in Xenopus., Lambert FM., Elife. May 30, 2018; 7
	An NMDAR positive and negative allosteric modulator series share a binding site and are interconverted by methyl groups., Perszyk R., Elife. May 24, 2018; 7
	Residues at the tip of the pore loop of NR3B-containing NMDA receptors determine Ca2+ permeability and Mg2+ block., Cavara NA., BMC Neurosci. October 19, 2010; 11 133.
	K(+) occupancy of the N-methyl-d-aspartate receptor channel probed by Mg(2+) block., Zhu Y., J Gen Physiol. March 1, 2001; 117 (3): 287-98.
	Na(+) occupancy and Mg(2+) block of the n-methyl-d-aspartate receptor channel., Zhu Y., J Gen Physiol. March 1, 2001; 117 (3): 275-86.
	Use of trifluoroperazine isolates a [(3)H]Ifenprodil binding site in rat brain membranes with the pharmacology of the voltage-independent ifenprodil site on N-methyl-D-aspartate receptors containing NR2B subunits., Coughenour LL., J Pharmacol Exp Ther. January 1, 2001; 296 (1): 150-9.
	Stoichiometry of recombinant N-methyl-D-aspartate receptor channels inferred from single-channel current patterns., Premkumar LS., J Gen Physiol. November 1, 1997; 110 (5): 485-502.
	Subconductance states of a mutant NMDA receptor channel kinetics, calcium, and voltage dependence., Premkumar LS., J Gen Physiol. February 1, 1997; 109 (2): 181-9.

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